Advanced Organic Chemistry

acetic acid acetone acetylene acid m.p. addition affords alcohol aldehyde alkali alkenes alkyl allyl amine anhydride aniline aqueous aromatic benzene boiling bromide carbon atoms carbonyl carbonyl group catalyst CH₂ CH2 CH2 CH₂OH CH3 CH3 CH3 CH3 H CO₂H compounds condensation converted COOH crystallization cyclohexane derivative diethyl distillation double bond electrons enol ester ethanol ether ethylene formation formula gives Grignard reagent H H H H₂O halide halogen heated HOCH hydrocarbon hydrogen chloride hydrolysis hydroxide hydroxyl hydroxyl group intermediate involves iodide isolated isomer isomerization ketone method methyl methyl group mixture mole molecular molecule naphthalene nitric nitric acid nitro nitrogen obtained OCH3 olefins optically active ortho oxidation oxygen Ph.D phenol potassium prepared quinone reaction reactive reacts rearrangement reduction refluxing resonance ring salt sodium soluble solution solvent stable structure substance substitution sulfonation sulfuric acid synthesis temperature tion trans Univ unsaturated yield он